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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

69306 — IVDR Class A IVDR by DIAGAST

MD Atlas
DIAGAST

EUDAMED last updated this device on Apr 27, 2026

69306

3661562AEMTDILXXXXXXXXXH9

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: DIAGAST
UDI-DI code: 23661562693065
Reference / catalog number: 69306

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Manufacturer information

Organization name: DIAGAST
SRN: FR-MF-000012310
Manufacturer status: Active

Critical warnings

8 warnings recorded — scroll inside the panel to see all entries.

CW083
EUDAMED did not publish a description for this code.
CW106
EUDAMED did not publish a description for this code.
CW159
EUDAMED did not publish a description for this code.
CW166
EUDAMED did not publish a description for this code.
CW167
EUDAMED did not publish a description for this code.
CW306
EUDAMED did not publish a description for this code.
CW999
P362+364 Take-off contaminated clothing and wash it before reuse.
CW999
P501 Dispose of contents/container in accordance with the local regulations, regional, national and international.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 23661562693065
Basic UDI-DI: 3661562AEMTDILXXXXXXXXXH9
Reference / catalog number: 69306
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0103030399ANTIBODY DETECTION (IMMUNOHAEMATOLOGY) - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.